JP5105706B2 - Thermoplastic resin composition, polymer composition, and molded article comprising the composition - Google Patents

Abstract

A thermoplastic resin composition (Y) characterized by comprising (A) 20 to 64.9 wt% one or more ethylene copolymers comprising an ethylene/±-olefin copolymer, (B) 35 to 70 wt% metal hydroxide, and (C) 0.1 to 30 wt% grafted ethylene polymer. The resin composition has excellent flame retardancy and has satisfactory pliability/flexibility and excellent tensile properties. It is suitable for use as an insulating material or sheath for electric wires. Also provided are: a polymer composition (Z) having high flame retardancy, characterized by comprising relative to (AA) 100 parts by weight of a polymer such as a thermoplastic polymer or thermosetting polymer, in the ratio of (BB) 50 to 250 parts by weight of a metal hydroxide, (E) 0.1 to 40 parts by weight of a triazine ring containing compound, and (F) 0.1 to 40 parts by weight of a polyhydric alcohol; and a molded object obtained from the polymer composition. These are suitable for use as an insulating material or sheath for electric wires.

Description

The present invention relates to a thermoplastic resin composition and a molded body thereof, and more specifically, a thermoplastic resin composition suitable as a wire insulator and a sheath material, a polymer composition having a high degree of flame retardancy, and the like It relates to a molded body consisting of

  Conventionally, polyvinyl chloride (PVC) has been frequently used as a sheath material and a part of an insulating material for electric wires, and its flexibility, flame retardancy, and insulation have been evaluated. Since PVC generally contains a lot of plasticizers, it tends to harden when it disappears due to heating, etc., and generates chlorine-based gas at the time of combustion. It came to be able to.

Under such circumstances, various flame retardant resin compositions based on ethylene-based polymers such as polyethylene have been proposed.
USP 6,232,377 includes a specific ethylene copolymer selected from ethylene / vinyl ester copolymer, ethylene / α, β-unsaturated carboxylic acid copolymer, low density polyethylene, etc. A flame retardant resin composition comprising an oxide, a triazine compound and a specific flame retardant compound is described. However, these ethylene-based polymers have a problem that flexibility and flexibility tend to decrease when the amount of an inorganic compound such as a metal hydroxide is increased in order to increase the flame retardancy.

  Accordingly, a resin composition having excellent flame retardancy, excellent flexibility and flexibility, and excellent tensile properties, and a molded body made of the composition, particularly an insulator and / or sheath for an electric wire are provided. This is the first object of the present invention.

  On the other hand, various thermoplastic polymers and thermosetting polymers are used in household electrical products, buildings, interior decorations, automobile parts, internal wiring of electronic devices, and the like. Most of these polymers (especially olefin polymers) are flammable.

From the standpoint of disaster prevention, there is a growing demand for non-flammable and flame-retardant facilities and structures, especially those that can be a source of fire, such as household electrical appliances, that require a high level of flame resistance. It is said that. The standard of flame retardancy of internal wiring materials is, for example, the UL standard (Underwriters La
boratories Inc. ) Etc., and is evaluated in a vertical combustion test called a VW-1 test. Therefore, there is a demand for materials that can withstand long-term use even when exposed to high heat or fire, and in order to impart high flame retardancy to many thermoplastic polymers and thermosetting polymers, polymers are required. A method of adding a flame retardant at the time of production or production of a molded product is widely adopted.

  Many flame retardants are used such as metal hydroxides; borates; organic halides; phosphorous compounds such as phosphates, red phosphorus and organic phosphorus compounds; and organic nitrogen compounds. Of these, organic halogen compounds, organophosphorus compounds and the like exhibit excellent flame retardant effects.

  However, these halogen-containing compounds are thermally decomposed during resin molding to generate hydrogen halide, which causes problems such as deterioration of the resin itself, coloration, and generation of hydrogen halide in the event of a fire. is there.

  Conventionally, inorganic flame retardants such as aluminum hydroxide and magnesium hydroxide have been used as flame retardants containing no halogen. However, these inorganic compounds alone have a low flame retardant effect, and if they are not added in a large amount, sufficient effects cannot be expressed. If they are added in a large amount, the original physical properties of the resin may be impaired, and the range of use is limited. It was.

On the other hand, there are specific organic phosphorus compounds, specific organic nitrogen compounds, and the like as flame retardants which do not contain halogen and can obtain a relatively good flame retardant effect, and these are often put into practical use.
A representative example of conventional organophosphate flame retardants is triphenyl phosphate (hereinafter referred to as “TPP”). This compound has low heat resistance and high volatility. Is not suitable, and the range of use is particularly limited due to mold contamination during molding.

  Condensed phosphoric acid esters described in JP-B 51-19858, JP-A 59-202240 and the like are used as a flame retardant which lowers organic phosphorus. Although these are superior to TPP in heat resistance and low volatility, the flame retardant effect per phosphorus content does not exceed TPP, and it is necessary to add a large amount. For this reason, there has been a problem that the heat distortion temperature is greatly lowered.

  Also, many formulations using polyphosphate flame retardants such as polyphosphates such as ammonium polyphosphate and polyphosphate amides have been proposed (Japanese Patent Laid-Open Nos. 54-22450, 9-316250, etc.) ). However, polyphosphoric acid is water-absorbing, and its electrical resistance gradually decreases due to water absorption, so its use is limited, such as being unsuitable for insulating coating materials such as electric wires and cables.

Recently, in order to suppress eutrophication of closed water systems such as lakes, prescriptions to replace phosphorus flame retardants are also required.
Organic nitrogen compounds such as melamine also exhibit a relatively high flame retardant effect (JP-A-8-176343, etc.). However, conventionally, in order to aim for a higher flame retardant effect, it has often been used in combination with a phosphorus-based flame retardant.

Accordingly, it is possible to provide a polymer composition having a high degree of flame retardancy without containing a halogen flame retardant or a phosphorus flame retardant, particularly a flame retardant polymer composition suitable as a coating material for a wire or a sheath. This is the second object of the present invention.
USP 6,232,377 Japanese Patent Publication No.51-19858 JP 59-202240 A Japanese Patent Laid-Open No. 54-22450 JP-A-9-316250 JP-A-8-176343

To provide a resin composition having excellent flame retardancy, flexibility and flexibility, and excellent tensile physical properties, and a molded body comprising the composition, particularly an electric wire insulator and / or sheath. Is the first object of the present invention.
It is possible to provide a polymer composition having a high degree of flame retardancy without containing a halogen flame retardant or a phosphorus flame retardant, particularly a flame retardant polymer composition suitable as a coating material for a wire or a sheath. It is the second object of the invention.

The polymer composition (Z) of the present invention is based on 100 parts by weight of at least one polymer (AA) selected from the thermoplastic polymer (aa1) and the thermosetting polymer (aa2).
Metal hydroxide (BB): 50 to 250 parts by weight of triazine compound (E): 0.1 to 40 parts by weight polyhydric alcohol (F): 0.1 to 40 in a proportion of parts,
The weight ratio of the triazine compound (E) and the polyhydric alcohol (F) is in the range of the following formula (1) .
(F) / (E) ≧ 1 (1)
As the polymer composition (Z), the thermoplastic polymer (aa1) is preferably an ethylene polymer.

The molded product of the present invention is characterized by comprising the polymer composition (Z).
In the present invention, the molded body is preferably an electric wire insulator. Moreover, it is preferable that the said molded object is a sheath of an electric wire.

  According to the present invention, a thermoplastic resin composition (Y) that exhibits excellent strength at break and elongation at break and is excellent in flexibility, flexibility, scratch resistance, and bending whitening resistance, and The molded body can be provided.

  Since the thermoplastic resin composition (Y) according to the present invention has the effects as described above, various molded products such as wire coatings, tapes, films, flame retardant sheets, pipes, blow molded products, flame retardant wallpaper and the like. It is suitable for an application, and is particularly suitable for an application of an electric wire covering such as an electric wire sheath and an electric wire insulator.

According to the present invention, it is possible to provide a polymer composition (Z) having a high degree of flame retardancy and a molded product thereof.
Since the polymer composition (Z) according to the present invention has the effects as described above, it is suitable for uses such as various molded products, for example, electric wire coatings, tapes, films, sheets, pipes, blow molded products, etc. It is suitable for wire coating applications such as wire sheaths and wire insulators.

Hereinafter, the thermoplastic resin composition (Y), the polymer composition (Z), the molded article made of the composition, and the uses thereof according to the present invention will be specifically described.
[Thermoplastic resin composition (Y)]
The thermoplastic resin composition (Y) according to the present invention is:
(A-1): an ethylene / α-olefin copolymer composed of ethylene and an α-olefin having 3 to 10 carbon atoms;
(A-2): An ethylene copolymer comprising an ethylene polymer other than (A-1) in a weight ratio of (A-1) / (A-2) = 20/80 to 100/0. (A) 20-64.9% by weight;
(B) 35 to 70% by weight of metal hydroxide,
(C) Graft-modified ethylene polymer 0.1 to 30% by weight
It is characterized by consisting of.

[(A) Ethylene copolymer]
The ethylene copolymer of the present invention comprises an ethylene / α-olefin copolymer (A-1) and an ethylene polymer (A-2) other than (A-1) (A-1) / (A- 2) = 20/80 to 100/0, preferably 50/50 to 100/0, more preferably 70/30 to 100/0. In addition, (A-1) and (A-2) which comprise ethylene-type copolymer (A) by this invention should just be contained in the thermoplastic resin composition (Y), (A-1) and A composition may be produced in advance from (A-2) to produce a thermoplastic resin composition (Y), and when producing a thermoplastic resin composition (Y), (A-1 ) And (A-2) may be added separately.

[(A-1) ethylene / α-olefin copolymer]
The ethylene / α-olefin copolymer (A-1) used in the present invention is a copolymer of ethylene and an α-olefin having 3 to 10 carbon atoms. Specific examples of the α-olefin having 3 to 10 carbon atoms include propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl-1-butene, 3-methyl-1-pentene, and 3-ethyl. -1-pentene, 4-methyl-1-pentene, 4-methyl-1-hexene, 4,4-dimethyl-1-pentene, 4-ethyl-1-hexene 1-octene, 3-ethyl-1-hexene, Examples include 1-octene and 1-decene, and the copolymer is composed of ethylene alone or in combination of two or more thereof. Of these, at least one of propylene, 1-butene, 1-hexene and 1-octene is preferably used.

  The content of each structural unit in the ethylene / α-olefin copolymer is usually 75 to 95 mol%, preferably 80 to 95 mol%, and the content of structural units derived from ethylene is α of 3 to 10 carbon atoms. -It is preferable that the content of the structural unit derived from at least one compound selected from olefins is usually 5 to 25 mol%, preferably 5 to 20 mol%.

Further, the ethylene / α-olefin copolymer (A-1) used in the present invention preferably has the following properties. That is,
(I) Density is 855 to 910 kg / m ³ , preferably 0.857 to 0.890 kg /
m ³
(Ii) Melt flow rate (MFR ₂ ) at 190 ° C. and a load of 2.16 kg is 0.
1-100 g / 10 min, preferably 0.1-20 g / 10 min.
(Iii) Index of molecular weight distribution evaluated by GPC method: Mw / Mn is in the range of 1.5 to 3.5, preferably 1.5 to 3.0, more preferably 1.8 to 2.5. More preferably (iv) the B value determined from the ¹³ C-NMR spectrum and the following formula is 0.9 to 1.5, preferably 1.0 to 1.2;
B value = [POE] / (2 · [PE] [PO])
(Wherein [PE] is the mole fraction of structural units derived from ethylene in the copolymer, and [PO] is the mole fraction of structural units derived from α-olefin in the copolymer. And [POE] is the ratio of the number of ethylene / α-olefin chains to the total number of dyad chains in the copolymer).

  This B value is an index representing the distribution of ethylene and the α-olefin having 3 to 10 carbon atoms in the ethylene / α-olefin copolymer. C. Randall (Macromolecules, 15, 353 (1982)), J. Am. It can be determined based on the report of Ray (Macromolecules, 10, 773 (1977)).

  As the B value is larger, the block chain of ethylene or α-olefin copolymer becomes shorter, the distribution of ethylene and α-olefin is more uniform, and the composition distribution of the copolymer rubber is narrower. In addition, as the B value becomes smaller than 1.0, the composition distribution of the ethylene / α-olefin copolymer becomes wider, and there are cases where there are bad points such as poor handling.

More preferably (v) the intensity ratio of Tαβ to Tαα (Tαβ / Tαα) in the ¹³ C-NMR spectrum is 0.5 or less, preferably 0.4 or less, more preferably 0.3 or less. Here, Tαα and Tαβ in the ¹³ C-NMR spectrum are peak intensities of CH _{2 in} the structural unit derived from an α-olefin having 3 or more carbon atoms, and the positions relative to the tertiary carbon are different as shown below. Two types of CH ₂ are meant.

このようなＴαβ／Ｔαα強度比は、下記のようにして求めることができる。エチレン・α−オレフィン共重合体の¹³Ｃ−ＮＭＲスペクトルを、たとえば日本電子（株）製ＪＥＯＬ−ＧＸ２７０ ＮＭＲ測定装置を用いて測定する。測定は、試料濃度５重量％になる
ように調整されたヘキサクロロブタジエン／ｄ６−ベンゼン＝２／１（体積比）の混合溶液を用いて、６７．８ＭＨｚ、２５℃、ｄ６−ベンゼン（１２８ｐｐｍ）基準で行う。測定された¹³Ｃ−ＮＭＲスペクトルを、リンデマンアダムスの提案（Ａｎａｌｙｓｉｓ Ｃ
ｈｅｍｉｓｔｒｙ，４３，ｐ１２４５（１９７１））、Ｊ．Ｃ．Ｒａｎｄａｌｌ（Ｒｅｖｉｅｗ Ｍａｃｒｏｍｏｌｅｃｕｌａｒ Ｃｈｅｍｉｓｔｒｙ Ｐｈｙｓｉｃｓ，Ｃ２９，
２０１（１９８９））に従って解析してＴαβ／Ｔαα強度比を求める。

Such a Tαβ / Tαα intensity ratio can be obtained as follows. The ¹³ C-NMR spectrum of the ethylene / α-olefin copolymer is measured using, for example, a JEOL-GX270 NMR measuring apparatus manufactured by JEOL Ltd. The measurement is performed using a mixed solution of hexachlorobutadiene / d6-benzene = 2/1 (volume ratio) adjusted to a sample concentration of 5% by weight, based on 67.8 MHz, 25 ° C., d6-benzene (128 ppm). To do. The measured ¹³ C-NMR spectrum was analyzed by Lindeman Adams' proposal (Analysis C
hemistry, 43, p1245 (1971)), J. Am. C. Randall (Review Macromolecular Chemistry Physics, C29,
201 (1989)) to obtain the Tαβ / Tαα intensity ratio.

As the ethylene / α-olefin copolymer of the present invention, those having the following properties in addition to the above properties are also preferably used.
(Vi) Ratio of melt flow rate (MFR ₁₀ ) at 190 ° C. and 10 kg load to melt flow rate (MFR ₂ ) at 190 ° C. and 2,16 kg load: MFR ₁₀ / MFR ₂ satisfies the following relationship.
MFR ₁₀ / MFR ₂ ≧ 5.7
Mw / Mn + 4.7 ≦ MFR ₁₀ / MFR ₂
Here, when MFR ₁₀ , MFR ₂ , and Mw / Mn do not satisfy the above relationship, the moldability and / or the material strength may decrease.

[Production Method of Ethylene / α-Olefin Copolymer (A-1)]
Such an ethylene / α-olefin copolymer (A-1) is composed of ethylene and at least one or more carbon atoms of 3 to 3 in the presence of a Ziegler catalyst or a metallocene catalyst composed of a V compound and an organoaluminum compound. Although it can manufacture by copolymerizing 10 alpha olefins, a metallocene catalyst is used suitably.

  Such a metallocene-based catalyst may be formed from the metallocene compound (a) and the compound (c) that reacts with the organoaluminum oxy compound (b) and / or the metallocene compound (a) to form an ion pair. Further, it may be formed from the organoaluminum compound (d) together with (a), (b) and / or (c).

The ethylene / α-olefin copolymerization can be carried out in a liquid phase using a hydrocarbon solvent in the presence of the above catalyst, and any of batch, semi-continuous and continuous methods. When a metallocene catalyst composed of a metallocene compound (a) and an organoaluminum oxy compound (b) or an ionized ionic compound (c) is used, the concentration of the metallocene compound (a) in the polymerization system is usually from about 0.00. 00005 to 0.1 mmol / liter (polymerization volume), preferably 0.0001 to 0.05 mmol / liter. The organoaluminum oxy compound (b) is supplied in an amount of 1 to 10,000, preferably 10 to 5,000, in terms of the molar ratio of aluminum atom to transition metal in the metallocene compound in the polymerization system (Al / transition metal). In the case of the ionized ionic compound (c), the molar ratio of the ionized ionic compound (c) to the metallocene compound (a) in the polymerization system (ionized ionic compound (c) / metallocene compound (a)) is 0.00. It is supplied in an amount of 5 to 20, preferably 1 to 10. When an organoaluminum compound is used, it is usually used in an amount of about 0 to 5 mmol / liter (polymerization volume), preferably about 0 to 2 mmol / liter.

The copolymerization reaction is usually performed at a reaction temperature of −20 to + 150 ° C., preferably 0 to 120 ° C., more preferably 0 to 100 ° C., and a pressure exceeding 0 to 7.8 MPa (80 kgf / cm ² , gauge pressure). Hereinafter, it is preferably carried out under the condition of more than 0 and 4.9 MPa (50 kgf / cm ² , gauge pressure) or less.

  Ethylene and α-olefin are supplied to the polymerization system in such an amount that the ethylene / α-olefin copolymer (A-1) having the specific composition is obtained. In the copolymerization, a molecular weight regulator such as hydrogen can be used.

[Ethylene polymer (A-2)]
The ethylene polymer (A-2) used in the present invention is an ethylene polymer other than (A-1), which is a linear low density polyethylene, a high pressure method low density polyethylene, ethylene / vinyl acetate copolymer Polymer, ethylene / ethyl acrylate copolymer, ethylene / methyl methacrylate copolymer, ethylene / acrylic acid copolymer, ethylene / methacrylic acid copolymer and its ionomer, ethylene / methacrylate copolymer, ethylene / carbon number 3 20 α-olefin / non-conjugated polyene copolymer. (A-2) is preferably an ethylene copolymer other than (A-1).

The ethylene copolymer (A) used in the present invention may be silane-grafted.
The silane-grafted ethylene copolymer (A) is prepared using a vinylsilane compound and a peroxide in combination to promote silane grafting. In the present invention, the silane-grafted ethylene copolymer (A) is an ethylene copolymer (A), a metal hydroxide (B), an unsaturated carboxylic acid or a derivative thereof that is not silane-grafted. The graft-modified ethylene polymer (C), vinyl silane compound and peroxide can also be obtained by melt-mixing by various conventionally known methods. The resulting thermoplastic resin composition according to the present invention contains the produced silane-grafted ethylene copolymer (A).

As the vinyl silane compound, specifically,
Examples include γ-methacryloxypropyltrimethoxysilane, vinyltrimethoxysilane, vinyltriethoxysilane, vinyltributoxysilane, vinyltris (β-methoxyethoxysilane), vinyltriacetoxysilane, and methyltrimethoxysilane. Of these, γ-methacryloxypropyltrimethoxysilane, vinyltrimethoxysilane, and vinyltriethoxysilane are preferable. The vinylsilane compound is usually used in a proportion of 0.5 to 2.5% by weight, preferably 0.5 to 2% by weight, based on 100% by weight of the total of (A) + (B) + (C). In other words, the vinylsilane compound is usually 0.5 to 2.5 parts by weight, preferably 0.5 to 2 parts by weight, based on 100 parts by weight of the total of (A) + (B) + (C). Used in proportions. When the vinyl silane compound is used in the above proportion, the silane grafting speed is high and an appropriate degree of silane grafting is obtained, and as a result, a molded article having an excellent balance between tensile elongation and tensile breaking point strength, for example, a wire coating layer is formed. can do.

In the present invention, as described above, the peroxide is used together with the vinyl silane compound in order to promote the silane graft reaction of the ethylene-based copolymer (A).
Such peroxides include organic peroxides, specifically
Benzoyl peroxide, dichlorobenzoyl peroxide, dicumyl peroxide, di-t-butyl peroxide, 2,5-dimethyl-2,5-di (peroxidebenzoate) hexyne-3, 1,4-bis (t-butylperoxyisopropyl) Benzene, lauroyl peroxide, t-butyl peroxide, 2,5-dimethyl-2,5-di- (t-butyl peroxide) hexyne-3, 2,5-dimethyl-2,5-di (t-butyl peroxide) Hexane, t-butyl perbenzoate, t-butyl perphenyl acetate, t-butyl perisobutyrate, t-butyl per-sec-octoate, t-butyl perpivalate, cumyl perpivalate, t-butyl perdiethyl acetate ; Azobisisobutyronitrile, dimethyl Zoisobuchireto and the like.

  Among these, dicumyl peroxide, di-t-butyl peroxide, 2,5-dimethyl-2,5-di (t-butylperoxy) hexyne-3, 2,5-dimethyl-2,5-di (t Dialkyl peroxides such as -butylperoxy) hexane and 1,4-bis (t-butylperoxyisopropyl) benzene are preferably used.

  The peroxide is usually 0.005 to 0.15% by weight, preferably 0.01 to 0.1% by weight with respect to the total of 100% by weight of (A) + (B) + (C). Used. In other words, the peroxide is usually 0.005 to 0.15 parts by weight, preferably 0.01 to 0.005 parts per 100 parts by weight of the total of (A) + (B) + (C). Used in a proportion of 1 part by weight. When the peroxide is used in the above proportion, the reaction of grafting the vinyl silane compound onto the ethylene copolymer (A) can be promoted moderately.

[Metal hydroxide (B)]
Examples of the metal hydroxide used in the present invention include aluminum hydroxide, magnesium hydroxide, calcium hydroxide, barium hydroxide, manganese hydroxide, zinc hydroxide, hydrotalcite alone or a mixture thereof. Particularly preferred are magnesium hydroxide alone and a mixture comprising magnesium hydroxide.

[Graft-modified ethylene polymer (C)]
As the ethylene polymer used as a raw material for the graft-modified ethylene polymer in the present invention, an ethylene / α-olefin copolymer is preferable. The ethylene / α-olefin copolymer used as a raw material for the graft-modified ethylene polymer is preferably a copolymer of ethylene and an α-olefin having 3 to 10 carbon atoms. Specific examples of the α-olefin having 3 to 10 carbon atoms include propylene, 1-butene, 1-pentene, 1-hexene, 3-methyl-1-butene, 3-methyl-1-pentene, and 3-ethyl. -1-pentene, 4-methyl-1-pentene, 4-methyl-1-hexene, 4,4-dimethyl-1-pentene, 4-ethyl-1-hexene, 1-octene, 3-ethyl-1-hexene , 1-octene, 1-decene and the like. These may be used alone or in combination of two or more. Of these, at least one of propylene, 1-butene, 1-hexene and 1-octene is particularly preferable.

  The content of each structural unit in the ethylene-based copolymer is such that the content of the structural unit derived from ethylene is usually 75 to 95 mol%, preferably 80 to 95 mol%, and α having 3 to 10 carbon atoms. -Content of the structural unit induced | guided | derived from the at least 1 compound chosen from an olefin is 5-25 mol% normally, and it is preferable that it is 5-20 mol%.

The ethylene / α-olefin copolymer used for graft modification preferably has the following physical properties. That is,
(I) Density is 855 to 910 kg / m ³ , preferably 857 to 890 kg / m ³ , (ii) Melt flow rate (MFR ₂ ) at 190 ° C. and 2.16 kg load is 0.1
-100 g / 10 min, preferably in the range of 0.1-20 g / 10 min,
(Iii) Index of molecular weight distribution evaluated by GPC method: Mw / Mn is in the range of 1.5 to 3.5, preferably 1.5 to 3.0, more preferably 1.8 to 2.5. ,
More preferably,
(Iv) B value calculated | required from a < ¹³ > C-NMR spectrum and a following formula is 0.9-1.5, Preferably it is 1.0-1.2;
B value = [POE] / (2 · [PE] [PO])
(Wherein [PE] is the mole fraction of structural units derived from ethylene in the copolymer, and [PO] is the mole fraction of structural units derived from α-olefin in the copolymer. And [POE] is the ratio of the number of ethylene / α-olefin chains to the total number of dyad chains in the copolymer).

  In addition, the ethylene / α-olefin copolymer used as a raw material for the graft-modified ethylene polymer has the same characteristics as those described for the ethylene / α-olefin copolymer used in (A-1). Although suitably used, the comonomer type, density, molecular weight, etc. of the copolymer may be the same as or different from (A-1).

  The graft-modified ethylene polymer according to the present invention can be obtained by graft-modifying the ethylene copolymer with a vinyl compound having at least one polar group. Examples of the vinyl compound having a polar group include vinyl compounds having an oxygen-containing group such as acid, acid anhydride, ester, alcohol, epoxy and ether as polar groups, vinyl compounds having a nitrogen-containing group such as isocyanate and amide, vinyl silane, etc. And vinyl compounds having a silicon-containing group.

Among these, vinyl compounds having an oxygen-containing group are preferable, and unsaturated epoxy monomers, unsaturated carboxylic acids and derivatives thereof are preferable.
Examples of the unsaturated epoxy monomer include unsaturated glycidyl ether and unsaturated glycidyl ester (for example, glycidyl methacrylate).

Examples of unsaturated carboxylic acids include acrylic acid, maleic acid, fumaric acid, tetrahydrophthalic acid, itaconic acid, citraconic acid, crotonic acid, isocrotonic acid and nadic acid ^TM (endocis-bicyclo [2,2,1] hept-5 -Ene-2,3-dicarboxylic acid) and the like.

  Examples of unsaturated carboxylic acid derivatives include acid halide compounds, amide compounds, imide compounds, acid anhydrides, and ester compounds of the above unsaturated carboxylic acids. Specific examples include maleyl chloride, maleimide, maleic anhydride, citraconic anhydride, monomethyl maleate, dimethyl maleate, and glycidyl maleate.

Of these, unsaturated dicarboxylic acids or acid anhydrides thereof are preferred, and maleic acid, nadic acid ^TM or acid anhydrides thereof are particularly preferred. The graft position of the unsaturated carboxylic acid or derivative thereof grafted to the unmodified ethylene copolymer is not particularly limited, and any carbon atom of the ethylene polymer constituting the graft modified ethylene polymer can be used. It is sufficient that an unsaturated carboxylic acid or a derivative thereof is bound to.

The graft-modified ethylene polymer (C) as described above can be prepared using various conventionally known methods, for example, the following methods.
(1) A method in which the unmodified ethylene polymer is melted with an extruder or the like, and an unsaturated carboxylic acid or the like is added to carry out graft copolymerization.
(2) A method in which the unmodified ethylene polymer is dissolved in a solvent and an unsaturated carboxylic acid or the like is added to carry out graft copolymerization.

In any method, it is preferable to perform the graft reaction in the presence of a radical initiator in order to efficiently graft copolymerize the above-mentioned unsaturated carboxylic acid or other graft monomer.
As the radical initiator, an organic peroxide, an azo compound, or the like is used. Specific examples of such radical initiators include organic peroxides such as benzoyl peroxide, dichlorobenzoyl peroxide, and dicumyl peroxide; azo compounds such as azobisisobutylnitrile and dimethylazoisobutyrate. Among these, dicumyl peroxide, di-tert-butyl peroxide, 2,5-dimethyl-2,5-di (tert-butylperoxy) hexyne-3, 2,5-dimethyl-2,5-di (tert Dialkyl peroxides such as -butylperoxy) hexane and 1,4-bis (tert-butylperoxyisopropyl) benzene are preferably used.

  These radical initiators are usually 0.001-1 part by weight, preferably 0.003-0.5 part by weight, more preferably 0.05-0, based on 100 parts by weight of the unmodified ethylene polymer. Used in an amount of 3 parts by weight.

  The reaction temperature in the graft reaction using the radical initiator as described above or the graft reaction performed without using the radical initiator is usually set in the range of 60 to 350 ° C, preferably 150 to 300 ° C.

[Other additives]
In addition to the above, the thermoplastic resin composition according to the present invention includes, as necessary, an antioxidant, an ultraviolet absorber, a weathering stabilizer, a heat stabilizer, an antistatic agent, a flame retardant, a pigment, a dye, and a lubricant. Etc. can be mix | blended. The blending amount may be determined according to the purpose. For example, when using a flame retardant typified by a silicone resin or the like, about 0.1 to 10 parts by weight can usually be used with respect to a total of 100 parts by weight of (A) + (B) + (C). .

[Thermoplastic resin composition]
The content of each component in the thermoplastic resin composition of the present invention is such that the lower limit of the content of the ethylene copolymer (A) is 20% by weight, preferably 25% by weight, more preferably 30% by weight. Is 64.9% by weight, preferably 60% by weight, more preferably 59.9% by weight, still more preferably 55% by weight. Moreover, the minimum of the content rate of a metal hydroxide (B) is 35 weight%, Preferably it is 40 weight%, and an upper limit is 70 weight%. The lower limit of the content ratio of the graft-modified ethylene polymer (C) is 0.1% by weight, and the upper limit is 30% by weight, preferably 10% by weight, more preferably 6% by weight. As a specific range, for example, the ethylene copolymer (A) is 20 to 64.9% by weight, preferably 25 to 60% by weight, and more preferably 30 to 55% by weight. The product (B) is 35 to 70% by weight, preferably 40 to 70% by weight, and the graft-modified ethylene polymer (C) is 0.1 to 30% by weight, preferably 0.1 to 10% by weight. The proportion is preferably 0.1 to 6% by weight. (When (A) + (B) + (C) = 100 wt%).

  In the present invention, when the total of (A), (B), and (C) is 100 parts by weight, 0.1 to 20 parts by weight of a triazine compound (E) as described later is added to polyhydric alcohol. A mode in which 0.1 to 20 parts by weight of (F) is added is preferable. The triazine compound (E) is a compound containing a triazine ring, which is melamine, ammelin, melam, benzguanamine, acetoguanamine, phthalodiguanamine, melamine cyanurate, melamine pyrophosphate, butylenediguanamine, norbornene diguanamine Methylene dimelamine, ethylene dimelamine, trimethylene dimelamine, tetramethylene dimelamine, hexamethylene dimelamine, 1,3-hexylene dimelamine and the like, and melamine cyanurate is particularly preferable.

  Examples of the polyhydric alcohol (F) include pentaerythritol, dipentaerythritol, tripentaerythritol, polypentaerythritol, trishydroxyethyl isocyanate, polyethylene glycol, glycerin, starch, glucose, cellulose, sorbitol and the like.

Here, when the weight ratio (E) / (F) of the triazine compound (E) and the polyhydric alcohol (F) is preferably 1 or more, the flame retardant effect is further enhanced.
The thermoplastic resin composition (Y) according to the present invention is obtained by melt-mixing the above-described components (A), (B) and (C) and additives that are blended as necessary by various conventionally known methods. To be prepared.

  For example, the above components are mixed simultaneously or sequentially into, for example, a Henschel mixer, a V-type blender, a tumbler mixer, a ribbon blender, etc., and then a single-screw extruder, a multi-screw extruder, a kneader, a Banbury mixer It can be obtained by melt-kneading with the above.

Among these, when a device excellent in kneading performance such as a multi-screw extruder, a kneader, and a Banbury mixer is used, a high-quality polymer composition in which each component is more uniformly dispersed can be obtained.
Moreover, the said additive, for example, antioxidant etc., can also be added as needed in these arbitrary steps.

[Polymer composition (Z)]
Next, the polymer composition (Z) according to the present invention will be described.
The polymer composition (Z) according to the present invention is based on 100 parts by weight of at least one polymer (AA) selected from the thermoplastic polymer (aa1) and the thermosetting polymer (aa2).
Metal hydroxide (BB): 50 to 250 parts by weight Triazine compound (E): 0.1 to 40 parts by weight Polyhydric alcohol (F): 0.1 to 40 parts by weight Yes.

  The polymer (AA) used in the polymer composition of the present invention is at least one polymer selected from a thermoplastic polymer (aa1) and a thermosetting polymer (aa2). These may be used alone or in combination.

[Thermoplastic polymer (aa1)]
Examples of thermoplastic polymers include olefin polymers such as ethylene polymers, propylene polymers, polybutene, and poly-4-methyl 1-pentene; styrene block copolymers; polyvinyl acetate; polyacrylates, polyacrylonitrile, and the like. Acrylic polymers; Polyethers such as polyphenylene oxide and polyethylene oxide; Polyesters such as PET; Polyurethanes; Polyamides; Polyphenylene sulfides; ABS resins; Polycarbonates; These may be used alone or in combination. Of these, ethylene polymers and styrene block copolymers are preferred.

  Examples of ethylene polymers include ethylene / α-olefin copolymers, ethylene / vinyl acetate copolymers, ethylene / ethyl acrylate copolymers, ethylene / methyl methacrylate copolymers, ethylene / acrylic acid copolymers, ethylene / acrylic acid copolymers, Examples thereof include methacrylic acid copolymers and their ionomers, ethylene / methacrylate copolymers, graft-modified ethylene / α-olefin copolymers, and the like. The molecular structure may be linear or branched having long or short side chains. These polymers may be a mixture with polyethylene.

  In the case of an ethylene / α-olefin copolymer, the α-olefin used as a comonomer is an α-olefin having 3 to 20 carbon atoms, preferably 3 to 10 carbon atoms, and is a random copolymer with ethylene. is there. Specific examples of α-olefins include propylene, 1-butene, 1-pentene, 1-hexene, 4-methylpentene-1, 1-octene, 1-decene, 1-dodecene and combinations thereof. Of these, propylene, 1-butene, 1-hexene and 1-octene are preferable. If necessary, other comonomers such as dienes such as 1,6-hexadiene, 1,8-octadiene, 5-ethylidene-2-norbornene and dicyclopentadiene, and cyclic olefins such as cyclopentene are contained in a small amount. May be. The ethylene content in the copolymer is 30 to 99.9 (mol%), preferably 50 to 99.5 (mol%), more preferably 75 to 99.5 (mol%).

  Although there is no restriction | limiting in particular about the manufacturing method of the said ethylene polymer, A homopolymerization of ethylene or a copolymerization of ethylene and an alpha olefin is carried out using a radical polymerization catalyst, a Phillips catalyst, a Ziegler-Natta catalyst, or a metallocene catalyst. Can be manufactured.

  In particular, the ethylene-based polymer used in the polymer composition (Z) of the present invention is preferably an ethylene / α-olefin copolymer that can be used as the component (A-1) of the thermoplastic resin composition (Y). Used.

  Styrene block copolymers include styrene / butylene / styrene block copolymers, styrene / isoprene / styrene block copolymers, styrene / ethylene / butylene / styrene block copolymers, and styrene / ethylene / propylene / styrene block copolymers. And a styrene / butadiene / styrene block copolymer and water additives thereof.

[Thermosetting polymer (aa2)]
Examples of the thermosetting polymer of the present invention include phenol resin, urea resin, melamine resin, unsaturated polyester, epoxy resin, polyurethane, and silicone resin. These may be used alone or in combination.

[Metal hydroxide (BB)]
Examples of the metal hydroxide of the present invention include aluminum hydroxide, magnesium hydroxide, calcium hydroxide, barium hydroxide, manganese hydroxide, zinc hydroxide, hydrotalcite and the like. These metal hydroxides may be used alone or as a mixture thereof, and magnesium hydroxide alone and a mixture containing magnesium hydroxide are particularly preferable.

[Triazine compound (E)]
The triazine compound of the present invention is a compound containing a triazine ring, which is melamine, ammelin, melam, benzguanamine, acetoguanamine, phthalodiguanamine, melamine cyanurate, melamine pyrophosphate, butylenediguanamine, norbornene diguanamine Methylene dimelamine, ethylene dimelamine, trimethylene dimelamine, tetramethylene dimelamine, hexamethylene dimelamine, 1,3-hexylene dimelamine and the like, and melamine cyanurate is particularly preferable.

[Polyhydric alcohol (F)]
Examples of the polyhydric alcohol of the present invention include pentaerythritol, dipentaerythritol, tripentaerythritol, polypentaerythritol, trishydroxyethyl isocyanate, polyethylene glycol, glycerin, starch, glucose, cellulose, sorbitol and the like.

[Other additives]
In addition to the above, the polymer composition according to the present invention includes, as necessary, an antioxidant, an ultraviolet absorber, a weathering stabilizer, a heat stabilizer, an antistatic agent, a flame retardant, a pigment, a dye, a lubricant, and the like. Additives can be blended.

[Polymer composition]
The polymer composition (Z) of the present invention comprises at least one polymer (AA) selected from the thermoplastic polymer (aa1) and the thermosetting polymer (aa2): 100 parts by weight of metal hydroxide. 50 to 250 parts by weight of product (BB), preferably 70 to 200 parts by weight 0.1 to 40 parts by weight of triazine compound (E), preferably 10 to 30 parts by weight of polyhydric alcohol (F) 0.1 -40 parts by weight, preferably 10-30 parts by weight.

Furthermore, when the weight ratio (F) / (E) of the triazine compound (E) and the polyhydric alcohol (F) is preferably 1 or more, the flame retardant effect is further enhanced.
The polymer composition (Z) according to the present invention comprises the components (AA), (BB), (E), and (F), and additives that are blended as necessary, in various conventionally known methods. It is prepared by melt mixing.

  For example, the polymer composition according to the present invention is prepared by mixing the above-mentioned components simultaneously or sequentially into, for example, a Henschel mixer, a V-type blender, a tumbler mixer, a ribbon blender, etc. It is obtained by melt-kneading with a multi-screw extruder, kneader, Banbury mixer or the like.

Among these, when a device excellent in kneading performance such as a multi-screw extruder, a kneader, and a Banbury mixer is used, a high-quality polymer composition in which each component is more uniformly dispersed can be obtained.
Moreover, the said additive, for example, antioxidant etc., can also be added as needed in these arbitrary steps.

[Molded body made of thermoplastic resin composition (Y) or polymer composition (Z)]
The molded body according to the present invention is obtained by the above-described method using the thermoplastic resin composition (Y) or the polymer composition (Z) according to the present invention, and a conventionally known melt molding method such as extrusion molding, It can be formed into various shapes by methods such as rotational molding, calendar molding, injection molding, compression molding, transfer molding, powder molding, blow molding, and vacuum molding.

  When the thermoplastic resin composition (Y) or the polymer composition (Z) according to the present invention is used for wire covering applications such as a wire sheath or a wire insulator, the molded body according to the present invention has a wire sheath. And a coating layer such as a wire sheath or a wire insulator is formed around the wire by a conventionally known method such as extrusion.

EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples.
The physical properties of the ethylene / α-olefin copolymer (A-1) and Tuffmer A described later were evaluated as follows.

(1) Density The strand after MFR measurement at 190 ° C. and a load of 2.16 kg was heat-treated at 120 ° C. for 1 hour, gradually cooled to room temperature over 1 hour, and then measured by a density gradient tube method.
(2) α-olefin content, Tαβ / Tαα, B value
Determined by ¹³ C-NMR spectrum.
(3) Intrinsic viscosity [η]
Measurements were made at 135 ° C. in decalin.
(4) Mw / Mn
GPC (gel permeation chromatography) was used and measured at 140 ° C. with an orthodichlorobenzene solvent.
(5) MFR ₁₀ / MFR ₂
According to ASTM D-1238, MFR ₁₀ at 10 ° C load at 190 ° C, 2
. The MFR ₂ at a load of 16 kg was measured and the ratio was calculated. When this ratio is large, it indicates that the fluidity at the time of melting of the polymer is excellent, that is, the processability is high.
Moreover, preparation of the sample of an insulated wire and its evaluation were performed by the following method.
(6) Strength at break and elongation at break In accordance with JIS K6301, a tensile test was performed using a JIS No. 3 dumbbell with a span of 20 mm and a tensile speed of 200 mm / min, and the strength at break and elongation at break were measured. .
(7) Torsional rigidity A torsional rigidity at a temperature of 23 ° C. was measured in accordance with JIS K6745 using a Crushberg type flexibility tester manufactured by Toyo Seiki Co., Ltd.
(8) Scratch resistance Using a Martens hardness scratch hardness tester manufactured by Tokyo Henki Co., Ltd., a groove width generated when a sample is scratched by applying a load of 20 g of a scratching indenter to a test piece having a thickness of 3 mm, The reciprocal was calculated and evaluated. An evaluation value of 11 or more was evaluated as ◯, 10 or more and less than 11 as Δ, and less than 10 as x.
(9) Bending-resistant whitening One end of a 2 mm thick test piece was fixed, and the end corresponding to the opposite face was bent 120 degrees or more perpendicularly from the end around a portion of 3 cm to check whether it was whitened. As evaluation, the thing which does not whiten was set to (circle) and the thing which whitens was set to x.

(Preparation of ethylene / 1-butene copolymer)
[Production Example 1]
(Preparation of catalyst solution)
0.63 mg of bis (1,3-dimethylcyclopentadienyl) zirconium dichloride is placed in a glass flask thoroughly purged with nitrogen, and 1.57 ml of a toluene solution of methylaminoxan (Al; 0.13 mmol / liter). And 2.43 ml of toluene were added to obtain a catalyst solution.

(Preparation of ethylene / 1-butene copolymer a-1)
912 ml of hexane and 200 ml of 1-butene were inserted into a 2 liter stainless steel autoclave sufficiently purged with nitrogen, and the temperature inside the system was raised to 80 ° C. Subsequently, 0.9 mmol of triisobutylaluminum and 2.0 ml of the catalyst solution prepared as described above (0.0005 mmol as Zr) were injected with ethylene to initiate polymerization. Polymerization was carried out at 80 ° C. for 30 minutes while maintaining a total pressure of 8.0 kg / cm ² -G by continuously supplying hydrogen at 70 ml / h and ethylene.

  A small amount of ethanol was introduced into the system to stop the polymerization, and then unreacted ethylene was purged. The obtained polymer was poured into a large excess of methanol to precipitate the polymer. The polymer was collected by filtration and dried overnight under reduced pressure to obtain an ethylene / 1-butene copolymer. Table 1 shows the properties of the obtained ethylene / 1-butene copolymer.

［製造例２］
（触媒溶液の調製）
トリフェニルカルベニウム（テトラキスペンタフルオロフェニル）ボレートを１８．４ｍｇとり、トルエンを５ｍｌ加えて溶解させ、濃度が０．００４ｍＭ／ｍｌのトルエン溶液を調製した。［ジメチル(ｔ−ブチルアミド)(テトラメチル−η⁵−シクロペンタジエニル)シラン］チタンジクロライドを１．８ｍｇとり、トルエンを５ｍｌ加えて溶解させ、
濃度が０．００１ｍＭ／ｍｌのトルエン溶液を調製した。重合開始時においてはトリフェニルカルベニウム(テトラキスペンタフルオロフェニル)ボレートのトルエン溶液を０．３８ｍｌ、［ジメチル(ｔ−ブチルアミド)(テトラメチル−η⁵−シクロペンタジエニル)シ
ラン］チタンジクロライドのトルエン溶液を０．３８ｍｌとり、さらに希釈用のトルエンを４．２４ｍｌ加えて、トリフェニルカルベニウム（テトラキスペンタフルオロフェニル）ボレートがＢ換算で０．００２ｍＭ／Ｌに、［ジメチル（ｔ−ブチルアミド）（テトラメチル−η⁵−シクロペンタジエニル）シラン］チタンジクロリドがＴｉ換算で０．００
０５ｍＭ／Ｌとなるトルエン溶液を５ｍｌ調製した。

[Production Example 2]
(Preparation of catalyst solution)
18.4 mg of triphenylcarbenium (tetrakispentafluorophenyl) borate was taken and 5 ml of toluene was added and dissolved to prepare a toluene solution having a concentration of 0.004 mM / ml. [Dimethyl (t-butylamide) (tetramethyl-η ⁵ -cyclopentadienyl) silane] 1.8 mg of titanium dichloride was taken and 5 ml of toluene was added and dissolved.
A toluene solution having a concentration of 0.001 mM / ml was prepared. At the start of polymerization, 0.38 ml of a toluene solution of triphenylcarbenium (tetrakispentafluorophenyl) borate and a toluene solution of [dimethyl (t-butylamide) (tetramethyl-η ⁵ -cyclopentadienyl) silane] titanium dichloride 0.38 ml, and further 4.24 ml of dilution toluene was added, and triphenylcarbenium (tetrakispentafluorophenyl) borate was converted to 0.002 mM / L in terms of B, [dimethyl (t-butylamide) (tetramethyl -Η ⁵ -cyclopentadienyl) silane] titanium dichloride in terms of Ti is 0.00
5 ml of a toluene solution at 05 mM / L was prepared.

(Preparation of ethylene / 1-butene copolymer a-2)
750 ml of heptane was inserted at 23 ° C. into a SUS autoclave with a stirring blade having a capacity of 1.5 liters that had been sufficiently purged with nitrogen. In this autoclave, 10 g of 1-butene and 120 ml of hydrogen were inserted while rotating a stirring blade and cooling with ice. Next, the autoclave was heated to 100 ° C. and further pressurized with ethylene so that the total pressure was 6 KG. When the internal pressure of the autoclave reached 6KG, 1.0 ml of a 1.0 mM / ml hexane solution of triisobutylaluminum (TIBA) was injected with nitrogen. Subsequently, 5 ml of the catalyst solution prepared as described above was pressed into the autoclave with nitrogen to initiate polymerization. Thereafter, the temperature of the autoclave was adjusted to an internal temperature of 100 ° C. for 5 minutes, and ethylene was directly supplied so that the pressure became 6 kg. Five minutes after the start of polymerization, 5 ml of methanol was inserted into the autoclave by a pump to stop the polymerization, and the autoclave was depressurized to atmospheric pressure. 3 liters of methanol was poured into the reaction solution with stirring. The resulting polymer containing the solvent was dried at 130 ° C. for 13 hours at 600 torr to obtain 10 g of ethylene / butene copolymer a-2. Table 2 shows the properties of the obtained ethylene / 1-butene copolymer.

（無水マレイン酸グラフト変性エチレン・１−ブテン共重合体の調整）
［製造例３］
上記エチレン・１−ブテン共重合体１０ｋｇと無水マレイン酸５０ｇおよびジ−ｔｅｒｔ−ブチルペルオキシド３ｇを５０ｇのアセトンに溶解させた溶液とをヘンシェルミキサー中でブレンドした。

(Adjustment of maleic anhydride graft-modified ethylene / 1-butene copolymer)
[Production Example 3]
10 kg of the above ethylene / 1-butene copolymer was mixed with 50 g of maleic anhydride and 3 g of di-tert-butyl peroxide in 50 g of acetone in a Henschel mixer.

  Next, the blend obtained as described above was introduced from a hopper of a single screw extruder having a screw diameter of 40 mm and L / D = 26, extruded into a strand at a resin temperature of 260 ° C. and an extrusion rate of 6 kg / hour, and then water-cooled. And then pelletized to obtain a maleic anhydride graft-modified ethylene / 1-butene copolymer.

  After extracting unreacted maleic anhydride from the obtained graft-modified ethylene / 1-butene copolymer with acetone, the amount of maleic anhydride grafted in the graft-modified ethylene / 1-butene copolymer was measured. The graft amount was 0.43% by weight.

[ Reference Examples Y1-1, Y1-2, Y1-3, Y1-4, Y2, Comparative Reference Examples Y1-1, Y2-1, Y2-2]
Reference Examples Y1-1, Y1-2, Y1-3, Y1-4, Y2 and Comparative Reference Examples Y1-1, Y2-1, Y2-2 were prepared as the ethylene copolymer (A) by the above-described production method. As a graft-modified ethylene polymer of magnesium hydroxide, unsaturated carboxylic acid or a derivative thereof as a metal hydroxide, as shown in Reference Example Y1-1 in Table 3. , Y1-2, Y1-3, Y1-4, Y2, Comparative Reference Examples Y1-1, Y2-1, Y2-2 Unmodified copolymers and unmodified polyethylene described in Table 3 with maleic anhydride What was modified so as to have a graft amount of 1 was blended at the stated weight%, and melt-kneaded and granulated using a Banbury mixer at a resin temperature of 190 ° C. to obtain pellets of a thermoplastic resin composition. Using this thermoplastic resin composition, each physical property was evaluated by the method described above. The results are shown in Table 3.

The unmodified copolymers described in Reference Examples Y1-1 and Y2 are ethylene / 1-butene copolymers a-1 prepared by the above production method. The unmodified copolymer described in Reference Example Y1-2 is an ethylene / 1-butene copolymer a-2 produced by the above production method.

［実施例Ｚ１〜Ｚ４、比較例Ｚ１〜Ｚ１４］
エチレン系共重合体（三井化学株式会社製、商品名タフマー Ａ−１０８５、密度：８
８５ｋｇ／ｍ³、１９０℃、２．１６ｋｇ荷重におけるＭＦＲ：１．２ｇ／１０分)、水酸化マグネシウム、メラミンシアヌレート、ペンタエリスリトール、ホウ酸亜鉛を表４に記載した重量部で配合し、バンバリーミキサーを用い、樹脂温度１９０℃で溶融混練、造粒を行ない、重合体組成物のペレットを得た。

[Examples Z1 to Z4 , Comparative Examples Z1 to Z14 ]
Ethylene copolymer (Mitsui Chemicals, trade name Toughmer A-1085, density: 8
85 kg / m ³ , 190 ° C., MFR at a load of 2.16 kg: 1.2 g / 10 min), magnesium hydroxide, melamine cyanurate, pentaerythritol, zinc borate are blended in parts by weight listed in Table 4, and Banbury Using a mixer, melt kneading and granulation were performed at a resin temperature of 190 ° C. to obtain pellets of the polymer composition.

Using this polymer composition with a melt extruder (manufactured by Toyo Seiki Co., Ltd., product name: Laboplast Mill) provided with a wire coating die, a die temperature: 220 ° C., screw rotation: 30 rpm, extrusion amount: 1. 2. The periphery of a 7-strand conductor (outer diameter of about 1.35 mm) of an annealed copper wire having an element wire diameter of 0.45 mm at 6 to 1.8 kg / h is coated with a 0.8 mm-thick polymer composition to obtain a finished diameter of 3. A sample of 0 mm insulated wire was obtained.

[Vertical combustion test (VW-1)]
The flame resistance of the insulation coating of the obtained sample of the insulated wire was evaluated by the VW-1 vertical combustion test defined in the above UL standard. That is, as shown in FIG. 1, in the chamber 1 of the test apparatus, a 17-inch-long insulated wire 2 as a sample is installed vertically, and the kraft paper 3 is pasted at a position 13 inches above the lower end, Absorbent cotton 4 was placed below the insulated wire 2.

  Next, the burner 5 disposed in front of the insulated wire 2 is ignited, and the flame is 15 ° at a 70 ° angle at a position 3 inches above the lower end of the insulated wire 2 as shown by a one-dot chain line in the figure. Repeat the combustion operation to make flame contact for 5 seconds, and measure the number of seconds after the flame burned to the insulation coating extinguishes the flame of the burner 5, and the longest spread time Was recorded.

  Then, the above test was performed three times. (1) The longest fire spread time for each test was 60 seconds or less in all three times. (2) Kraft paper 3 was not burnt by fire spread from the insulation coating. (3 ) Absorbent cotton 4 does not burn due to burning fallen thing, those that satisfy all three conditions are good flame retardant (pass), those that do not satisfy any one as flame retardant failure (fail) evaluated. In addition, for those that failed to evaluate the flame retardancy, those that satisfied two of the three conditions (△), those that satisfied one of the three conditions (▲), those not satisfying all of the above three conditions were distinguished from (×). The results are shown in Table 4.

  For those that have failed, a pass can be expected by increasing the coating thickness according to the flame retardant hierarchy. Therefore, (Δ) can be expected to reach a passing level with a relatively small increase, while (▲) and (×) will require a considerably thicker coating.

［実施例Ｚ５〜Ｚ６、比較例Ｚ１５〜Ｚ１８］
タフマー Ａ−１０８５、水酸化マグネシウム、メラミンシアヌレート、ペンタエリス
リトール、ホウ酸亜鉛を表５に記載した重量部で配合し、バンバリーミキサーを用い、樹脂温度１９０℃で溶融混練、造粒を行ない、重合体組成物のペレットを得た。

[Examples Z5 to Z6 , Comparative Examples Z15 to Z18 ]
Tuffmer A-1085, magnesium hydroxide, melamine cyanurate, pentaerythritol, zinc borate are blended in parts by weight listed in Table 5, and are melt-kneaded and granulated at a resin temperature of 190 ° C. using a Banbury mixer. A pellet of the coalescence composition was obtained.

Using this polymer composition with a melt extrusion machine (product name: Laboplast Mill, manufactured by Toyo Seiki Co., Ltd.) equipped with a wire coating die, a die temperature: 220 ° C., screw rotation: 30 rp
m, extrusion rate: 1.6 to 1.8 kg / h, and a polymer composition having a thickness of 1.0 mm around a 7-strand conductor (outside diameter of about 4.8 mm) of an annealed copper wire having a strand diameter of 1.6 mm A sample of an insulated wire with a finished diameter of 6.8 mm was obtained by coating. And about the obtained sample, the vertical combustion test (VW-1) was done like the above. The results are shown in Table 5.

FIG. 1 is a partially cutaway perspective view of a VW-1 combustion test apparatus defined in the UL standard. In FIG. 1, the length a is 10 inches, the length b is 17 inches, the length c is 3 inches, the distance d is 1 and 1/2 inches, and the angle θ1 is 70 °. The angle θ2 is 20 °.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 ... Chamber 2 ... Insulated wire 3 ... Kraft paper 4 ... Absorbent cotton 5 ... Burner

Claims (5)

At least one polymer (AA) selected from the thermoplastic polymer (aa1) and the thermosetting polymer (aa2): with respect to 100 parts by weight,
Metal hydroxide (BB): 50 to 250 parts by weight Triazine compound (E): 0.1 to 40 parts by weight Polyhydric alcohol (F): 0.1 to 40 parts by weight
The polymer composition (Z), wherein the weight ratio of the triazine compound (E) and the polyhydric alcohol (F) is in the range of the following formula (1) and does not contain a halogen-based flame retardant or a phosphorus-based flame retardant. . (F) / (E) ≧ 1 (1)   The polymer composition (Z) according to claim 1, wherein the thermoplastic polymer (aa1) is an ethylene polymer.   A molded article comprising the polymer composition (Z) according to claim 1 or 2.   4. The molded body according to claim 3, wherein the molded body is an insulator of an electric wire.   The molded body according to claim 3, wherein the molded body is a sheath of an electric wire.

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